Variant Details

Variant: esv3306465

Internal ID

15153413

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr1:204375912..204375913	hg38	UCSC Ensembl
Inner	chr1:204375895..204375930	hg38	UCSC Ensembl
Outer	chr1:204375894..204375931	hg38	UCSC Ensembl
	chr1:204345040..204345041	hg19	UCSC Ensembl
Inner	chr1:204345023..204345058	hg19	UCSC Ensembl
Outer	chr1:204345022..204345059	hg19	UCSC Ensembl
	chr1:202611663..202611664	hg18	UCSC Ensembl
Inner	chr1:202611681..202611646	hg18	UCSC Ensembl
Outer	chr1:202611645..202611682	hg18	UCSC Ensembl

Cytoband

1q32.1

Allele length

Assembly	Allele length
hg38	301
hg19	301
hg18	301

Variant Type

CNV mobile element insertion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv7833114, essv7772169, essv7778123, essv7817114, essv7820396, essv7779343, essv7793804, essv7786552, essv7815918, essv7795665, essv7807188, essv7821221, essv7824206, essv7776915, essv7788390, essv7805335, essv7781583, essv7777319, essv7810735, essv7800198, essv7786332, essv7825635, essv7820044, essv7829638, essv7836236, essv7804211, essv7826556, essv7774090, essv7794337, essv7806640, essv7797090, essv7834961, essv7814954, essv7813425, essv7783686, essv7773766, essv7783735, essv7825095

Samples

NA18502, NA18861, NA10851, NA18980, NA11931, NA12751, NA18545, NA12004, NA18959, NA19190, NA18870, NA18940, NA18558, NA18916, NA11918, NA12828, NA11831, NA12489, NA18907, NA19114, NA11919, NA11894, NA19099, NA19225, NA18523, NA18858, NA18593, NA18945, NA12043, NA18608, NA11881, NA18961, NA19147, NA19143, NA19093, NA12006, NA12776, NA18577

Known Genes

Method

Sequencing

Analysis

Platform

Roche 454

Comments

Reference

1000_Genomes_Consortium_Pilot_Project

Pubmed ID

20981092

Accession Number(s)

esv3306465

Frequency

Sample Size	185
Observed Gain	38
Observed Loss	0
Observed Complex	0
Frequency	n/a